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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451696Generated: November 1, 2026

Sodium hydride → Methyl 5-methyl-2-((2-nitrophenyl)amino)thiophene-3-carboxylate

https://huagongshe.com/reaction/1451696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantMethyl-2-amino-5-methyl-3-thiophenecarboxylateHCID 675878—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 5-methyl-2-((2-nitrophenyl)amino)thiophene-3-carboxylateHCID 19592005—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred suspension of sodium hydride (2 g) in dry tetrahydrofuran (25 mL) under a nitrogen atmosphere was added a solution of methyl 2-amino-5-methylthiophene-3-carboxy-late (4.8 g, 0.028 mol) and 2-fluoronitrobenzene (4.0 g, 0.025 mol) in dry tetrahydrofuran (30 mL). The mixture was stirred at 25° C. for 20 hours, poured onto ice and partitioned between 2N hydrochloric acid and ethyl acetate. The organic extracts were dried over magnesium sulfate, the solvent was evaporated under reduced pressure and the title compound purified by chromatography on silica gel, eluted with toluene, and crystallized from ethanol (4.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05605897
Source datasetuspto-grants-1997_02
ORD IDord-03a006a3ccc346e7a32a73f772aeef17
Source noteuspto-grants-1997_02